Systemic autoimmune diseases in patients with hepatitis C virus infection: characterization of 1020 cases (The HISPAMEC Registry).

Objective. To describe the clinical and immunologic characteristics of a large series of patients with systemic autoimmune diseases (SAD) associated with chronic hepatitis C virus (HCV) infection. Methods. The HISPAMEC Registry is a multicenter international study group dedicated to collecting data...

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Fecha de publicación:
2009
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/27010
Acceso en línea:
https://doi.org/10.3899/jrheum.080874
https://repository.urosario.edu.co/handle/10336/27010
Palabra clave:
Hepatitis C Virus
Sjögren’s Syndrome
Systemic Lupus Erythematosus
Rheumatoid Arthritis
Polyarteritis Nodosa
Antiphospholipid Syndrome
Lymphoma
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id EDOCUR2_892866348a5219fbd30a2852983248ed
oai_identifier_str oai:repository.urosario.edu.co:10336/27010
network_acronym_str EDOCUR2
network_name_str Repositorio EdocUR - U. Rosario
repository_id_str
spelling 8e65e67d-e83d-4d5a-a74a-6b78eb76ea47-19db5cd18-7bf8-4c77-b4a1-df55bb01f233-1c6461ced-440b-4091-8bfc-8f97a006950a-18978090f-6e00-4fa7-af44-082256056c92-10aae4b9b-4bcb-4fa4-8c2f-b66290d047c5-10b35d229-3e80-4eea-bde7-c4845b5b2250-140e55f5c-20cd-4a40-ac31-112db5cec759-18e386080-ad94-431e-a60e-8570357d08c9-12020-08-19T14:40:45Z2020-08-19T14:40:45Z2009-01-16Objective. To describe the clinical and immunologic characteristics of a large series of patients with systemic autoimmune diseases (SAD) associated with chronic hepatitis C virus (HCV) infection. Methods. The HISPAMEC Registry is a multicenter international study group dedicated to collecting data on patients diagnosed with SAD with serological evidence of chronic HCV infection. The information sources are cases reported by physicians of the HISPAMEC Study Group and periodic surveillance of reported cases by a Medline search updated up to December 31, 2007. Results. One thousand twenty HCV patients with SAD were included in the registry. Patients were reported from Southern Europe (60%), North America (15%), Asia (14%), Northern Europe (9%), South America (1%), and Australia (1%). Countries reporting the most cases were Spain (236 cases), France (222 cases), Italy (144 cases), USA (120 cases), and Japan (95 cases). The most frequently reported SAD were Sjögren’s syndrome (SS; 483 cases), rheumatoid arthritis (RA; 150 cases), systemic lupus erythematosus (SLE; 129 cases), polyarteritis nodosa (78 cases), antiphospholipid syndrome (59 cases), inflammatory myopathies (39 cases), and sarcoidosis (28 cases). Twenty patients had 2 or more SAD. Epidemiological data were available in 677 cases. Four hundred eighty-seven (72%) patients were female and 186 (28%) male, with a mean age of 49.5 ± 1.0 years at SAD diagnosis and 50.5 ± 1.1 years at diagnosis of HCV infection. The main immunologic features were antinuclear antibody (ANA) in 61% of patients, rheumatoid factor (RF) in 57%, hypocomplementemia in 52%, and cryoglobulins in 52%. The main differential aspect between primary and HCV-related SAD was the predominance of cryoglobulinemic-related markers (cryoglobulins, RF, hypocomplementemia) over specific SAD-related markers (anti-ENA antibodies, anti-dsDNA, anti-cyclic citrullinated peptide) in patients with HCV. Conclusion. In the selected cohort, the SAD most commonly reported in association with chronic HCV infection were SS (nearly half the cases), RA and SLE. Nearly two thirds of SAD-HCV cases were reported from the Mediterranean area. In these patients, ANA, RF and cryoglobulins are the predominant immunological features. (First Release April 15 2009; J Rheumatol 2009;36:1442–8; doi:10.3899/jrheum.080874).application/pdfhttps://doi.org/10.3899/jrheum.080874ISSN: 0315-162XEISSN: 1499-2752https://repository.urosario.edu.co/handle/10336/27010engThe journal of rheumatology1448No. 71442Journal of RheumatologyVol. 36Journal of Rheumatology, ISSN:0315-162X ; EISSN: 1499-2752, Vol.36, No.7 (July 2009); pp. 1442-1448https://www.jrheum.org/content/jrheum/36/7/1442.full.pdfAbierto (Texto Completo)http://purl.org/coar/access_right/c_abf2Journal of Rheumatologyinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocURHepatitis C VirusSjögren’s SyndromeSystemic Lupus ErythematosusRheumatoid ArthritisPolyarteritis NodosaAntiphospholipid SyndromeLymphomaSystemic autoimmune diseases in patients with hepatitis C virus infection: characterization of 1020 cases (The HISPAMEC Registry).Enfermedades autoinmunes sistémicas en pacientes con infección por el virus de la hepatitis C: caracterización de 1020 casos (Registro HISPAMEC).articleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Ramos Casals, ManuelMuñoz, SandraMedina, FranciscoJara, Luis JavierRosas, JoséCalvo Alen, JaimeBrito Zenon, PilarSanchez Tapias, Jose Maria10336/27010oai:repository.urosario.edu.co:10336/270102022-05-02 07:37:21.86995https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv Systemic autoimmune diseases in patients with hepatitis C virus infection: characterization of 1020 cases (The HISPAMEC Registry).
dc.title.TranslatedTitle.spa.fl_str_mv Enfermedades autoinmunes sistémicas en pacientes con infección por el virus de la hepatitis C: caracterización de 1020 casos (Registro HISPAMEC).
title Systemic autoimmune diseases in patients with hepatitis C virus infection: characterization of 1020 cases (The HISPAMEC Registry).
spellingShingle Systemic autoimmune diseases in patients with hepatitis C virus infection: characterization of 1020 cases (The HISPAMEC Registry).
Hepatitis C Virus
Sjögren’s Syndrome
Systemic Lupus Erythematosus
Rheumatoid Arthritis
Polyarteritis Nodosa
Antiphospholipid Syndrome
Lymphoma
title_short Systemic autoimmune diseases in patients with hepatitis C virus infection: characterization of 1020 cases (The HISPAMEC Registry).
title_full Systemic autoimmune diseases in patients with hepatitis C virus infection: characterization of 1020 cases (The HISPAMEC Registry).
title_fullStr Systemic autoimmune diseases in patients with hepatitis C virus infection: characterization of 1020 cases (The HISPAMEC Registry).
title_full_unstemmed Systemic autoimmune diseases in patients with hepatitis C virus infection: characterization of 1020 cases (The HISPAMEC Registry).
title_sort Systemic autoimmune diseases in patients with hepatitis C virus infection: characterization of 1020 cases (The HISPAMEC Registry).
dc.subject.keyword.spa.fl_str_mv Hepatitis C Virus
Sjögren’s Syndrome
Systemic Lupus Erythematosus
Rheumatoid Arthritis
Polyarteritis Nodosa
Antiphospholipid Syndrome
Lymphoma
topic Hepatitis C Virus
Sjögren’s Syndrome
Systemic Lupus Erythematosus
Rheumatoid Arthritis
Polyarteritis Nodosa
Antiphospholipid Syndrome
Lymphoma
description Objective. To describe the clinical and immunologic characteristics of a large series of patients with systemic autoimmune diseases (SAD) associated with chronic hepatitis C virus (HCV) infection. Methods. The HISPAMEC Registry is a multicenter international study group dedicated to collecting data on patients diagnosed with SAD with serological evidence of chronic HCV infection. The information sources are cases reported by physicians of the HISPAMEC Study Group and periodic surveillance of reported cases by a Medline search updated up to December 31, 2007. Results. One thousand twenty HCV patients with SAD were included in the registry. Patients were reported from Southern Europe (60%), North America (15%), Asia (14%), Northern Europe (9%), South America (1%), and Australia (1%). Countries reporting the most cases were Spain (236 cases), France (222 cases), Italy (144 cases), USA (120 cases), and Japan (95 cases). The most frequently reported SAD were Sjögren’s syndrome (SS; 483 cases), rheumatoid arthritis (RA; 150 cases), systemic lupus erythematosus (SLE; 129 cases), polyarteritis nodosa (78 cases), antiphospholipid syndrome (59 cases), inflammatory myopathies (39 cases), and sarcoidosis (28 cases). Twenty patients had 2 or more SAD. Epidemiological data were available in 677 cases. Four hundred eighty-seven (72%) patients were female and 186 (28%) male, with a mean age of 49.5 ± 1.0 years at SAD diagnosis and 50.5 ± 1.1 years at diagnosis of HCV infection. The main immunologic features were antinuclear antibody (ANA) in 61% of patients, rheumatoid factor (RF) in 57%, hypocomplementemia in 52%, and cryoglobulins in 52%. The main differential aspect between primary and HCV-related SAD was the predominance of cryoglobulinemic-related markers (cryoglobulins, RF, hypocomplementemia) over specific SAD-related markers (anti-ENA antibodies, anti-dsDNA, anti-cyclic citrullinated peptide) in patients with HCV. Conclusion. In the selected cohort, the SAD most commonly reported in association with chronic HCV infection were SS (nearly half the cases), RA and SLE. Nearly two thirds of SAD-HCV cases were reported from the Mediterranean area. In these patients, ANA, RF and cryoglobulins are the predominant immunological features. (First Release April 15 2009; J Rheumatol 2009;36:1442–8; doi:10.3899/jrheum.080874).
publishDate 2009
dc.date.created.spa.fl_str_mv 2009-01-16
dc.date.accessioned.none.fl_str_mv 2020-08-19T14:40:45Z
dc.date.available.none.fl_str_mv 2020-08-19T14:40:45Z
dc.type.eng.fl_str_mv article
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_6501
dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.3899/jrheum.080874
dc.identifier.issn.none.fl_str_mv ISSN: 0315-162X
EISSN: 1499-2752
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/27010
url https://doi.org/10.3899/jrheum.080874
https://repository.urosario.edu.co/handle/10336/27010
identifier_str_mv ISSN: 0315-162X
EISSN: 1499-2752
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationEndPage.none.fl_str_mv 1448
dc.relation.citationIssue.none.fl_str_mv No. 7
dc.relation.citationStartPage.none.fl_str_mv 1442
dc.relation.citationTitle.none.fl_str_mv Journal of Rheumatology
dc.relation.citationVolume.none.fl_str_mv Vol. 36
dc.relation.ispartof.spa.fl_str_mv Journal of Rheumatology, ISSN:0315-162X ; EISSN: 1499-2752, Vol.36, No.7 (July 2009); pp. 1442-1448
dc.relation.uri.spa.fl_str_mv https://www.jrheum.org/content/jrheum/36/7/1442.full.pdf
dc.rights.coar.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.rights.acceso.spa.fl_str_mv Abierto (Texto Completo)
rights_invalid_str_mv Abierto (Texto Completo)
http://purl.org/coar/access_right/c_abf2
dc.format.mimetype.none.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv The journal of rheumatology
dc.source.spa.fl_str_mv Journal of Rheumatology
institution Universidad del Rosario
dc.source.instname.none.fl_str_mv instname:Universidad del Rosario
dc.source.reponame.none.fl_str_mv reponame:Repositorio Institucional EdocUR
repository.name.fl_str_mv Repositorio institucional EdocUR
repository.mail.fl_str_mv edocur@urosario.edu.co
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